Canonical Allele Identifier: PA179258
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166306
ClinVar RCV Id: RCV000152491 RCV000280983 RCV000296370 RCV000326911 RCV000349014 RCV000388430 RCV000534706 RCV001310766 RCV002415643 RCV003486685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr2690Ile
CA179255
NM_001267550.2:c.8069C>T